A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613764



Internal ID6653972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76500726..76515970hg38UCSC Ensembl
chr7:76130043..76145287hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3815245
hg1915245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848888, essv12848890, essv12848885, essv12848886, essv12848891, essv12848889, essv12848887
SamplesNA21123, NA20851, NA21098, NA19701, NA19681, NA20753, HG02860
Known GenesDTX2, UPK3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613764
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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